The X-ray crystal structure of the double-headed amphiphile (1S,2S)-1,2-bis(d-gluconamido)cyclohexane
✍ Scribed by Christoph André; Peter Luger; Daniel Nehmzow; Jürgen-Hinrich Fuhrhop
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 785 KB
- Volume
- 261
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
✦ Synopsis
If a mixture of diastereomeric and enantiomeric 1,2-diaminocyclohexanes is amidated with o-glucono-l,Mactone, only one of the four diasteroeomeric amides, namely the title compound, crystallizes from the mixture. The same amide was also synthesized and crystallized from enantiomerically pure S,S-diamino-cyclohexane.
The lR,2R-diamide was also synthesized, but could not be crystallized. (lS,2S)-1,2-bis(o-gluconamidokyclohexane, C,$!,,N,O,,,
📜 SIMILAR VOLUMES
Mono and Difunctionalization of Chiral Ferrocenyl Bisacetals. X-Ray Crystal Structure of Bis-1,1'-[(2S,4S)-(hydroxymethyl)-2-dioxane1,3]ferrocene. -The title chiral bisacetals (III) and (V) react with tBuLi and MeLi to the o-Li compounds, which are converted with electrophiles like (VI) to o-substit